Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42816961-42817145 | Common:1; Rare:52 | ||||
chr1:42817198-42817260 | Rare:18 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958801-42959042 | Common:3; Rare:65; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172164-43172377 | Common:3; Rare:89 | ||||
chr1:43300807-43301020 | Common:2; Rare:34 | ||||
chr1:43358662-43358986 | Common:7; Rare:102 | ||||
chr1:43367584-43367815 | Common:2; Rare:42 | ||||
chr1:43367927-43368208 | Rare:72 | ||||
chr1:43389742-43389966 | Common:4; Rare:102; Clinvar:1 | ||||
chr1:43530770-43530931 | Common:2; Rare:66 | ||||
chr1:43605429-43605586 | Common:1; Rare:60 | ||||
chr1:43707337-43707674 | Common:2; Rare:96 | ||||
chr1:43946585-43946983 | Rare:105 | ||||
chr1:43974862-43975058 | Common:3; Rare:61 |